| LMBB | Laurence-Moon-Bardet-Biedl [syndrome] |
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| BBS | BARDET-Biedl syndrome |
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| Bardet | Georges, French physician, *1885. See: Bardet-Biedl syndrome. (05 Mar 2000) |
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| Bardet-Biedl syndrome | <syndrome> Mental retardation, pigmentary retinopathy, polydactyly, obesity, and hypogenitalism; recessive inheritance. See: Laurence-Moon-Biedl syndrome. (05 Mar 2000) |
Synonyms : Bardet Biedl Syndrome, Laurence Moon Bardet Biedl Syndrome, Syndrome, Bardet-Biedl, Syndrome, Laurence-Moon-Bardet-Biedl
| Bardet-Biedl syndrome |
Inherited rare disorder. Characteristics of this syndrome include mental retardation, degeneration of the retinas of the eyes, kidney abnormalities, delayed sexual development or underdeveloped reproductive organs, obesity, and/or abnormal fingers and toes.
Ãâó: www.sparkle.usu.edu/glossary/syndromes_glossary.as...
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| Bardet-Biedl syndrome |
Mental retardation, pigmentary retinopathy, polydactyly, obesity, and hypogenitalism; recessive inheritance.
Ãâó: dragon.zoo.utoronto.ca/~B03T0801B/glossary.html
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| Bardet-Biedl syndrome |
A genetic disorder characterized by degeneration of the light sensitive cells in the periphery of the retina causing night blindness, tunnel vision, decreased visual acuity, and photophobia. Other conditions include obesity, developmental delays, spastic paraplegia and renal disorders.
Ãâó: www.visionrx.com/library/dictionary/eye_dictionary...
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| Bardet-Biedl s. |
an autosomal recessive disorder characterized by mental retardation, pigmentary retinopathy, obesity, polydactyly, and hypogonadism; cf. Laurence-Moon s. and Biemond s., II.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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